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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 19 Results
Recall Date to: 08/04/2015 PMA Number: P980016
 
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Medtronic EnTrust, Dual Chamber Implantable, Cardioverter Defibrillator with Atrial and Ventricular ... 2 03/22/2012 Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic EnTrust, Dual Chamber Implantable, Cardioverter Defibrillator with Ventricular Therapies, ... 2 03/22/2012 Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic EnTrust, Single Chamber Implantable, Cardioverter Defibrillator with Ventricular Therapies... 2 03/22/2012 Medtronic Inc. Cardiac Rhythm Disease Management
Medtronic GEM DR Implantable Cardioverter Defibrillators, Model 7271 1 07/20/2004 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Marquis DR, model 7274 Dual Chamber Implantable Cardioverter Defibrillator (ICD) devices a... 2 03/11/2005 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Marquis VR, model 7230 Single Chamber Implantable Cardioverter Defibrillator (ICD)devices ... 2 03/11/2005 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Maximo DR, model 7278 Single Chamber Implantable Cardioverter Defibrillator (ICD)devices a... 2 03/11/2005 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Maximo II DR D28DRG, for ventricular pacing and defibrillation. 2 01/28/2009 Medtronic Inc. Cardiac Rhythm Managment
Medtronic Maximo II DR, model D284DRG. Digital dual chamber implantable cardioverter defibrillator ... 2 10/21/2010 Medtronic Inc. Cardiac Rhythm Disease Managment
Medtronic Maximo II VR D284VRC, for ventricular pacing and defibrillation. 2 01/28/2009 Medtronic Inc. Cardiac Rhythm Managment
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